# Impact of finerenone on chronic kidney disease progression in Chinese patients with type 2 diabetes: a FIGARO-DKD subgroup analysis

**Authors:** Ping Li, Hongguang Zheng, Jianhua Ma, Weiping Lu, Ling Li, Fang Liu, Qing Su, Yuxiu Li, Yi Fang, Zhaohui Mo, Fei Xiong, Aiping Yin, Ying Zhang, Li Wang, Meike Brinker, Luke Roberts, Dalong Zhu

PMC · DOI: 10.3389/fendo.2025.1568438 · Frontiers in Endocrinology · 2025-04-30

## TL;DR

Finerenone reduces kidney disease progression in Chinese patients with type 2 diabetes and chronic kidney disease, with acceptable safety.

## Contribution

This study evaluates finerenone's efficacy and safety in Chinese patients with type 2 diabetes and CKD, a previously underrepresented population.

## Key findings

- Finerenone significantly reduced the risk of a key kidney outcome (hazard ratio 0.48).
- There was a trend toward reduced cardiovascular outcomes with finerenone (hazard ratio 0.91).
- Hyperkalemia incidence was high but hospitalization and discontinuation rates were low.

## Abstract

Type 2 diabetes (T2D) is a considerable and growing burden in the Chinese population, and affected adults are at high risk of developing chronic kidney disease (CKD). This subgroup analysis of the FIGARO-DKD trial explored the cardiovascular and kidney benefits of finerenone in Chinese patients with CKD and T2D on optimized renin–angiotensin system blockade.

Patients with urine albumin-to-creatinine ratio (UACR) ≥30–<300 mg/g and estimated glomerular filtration rate (eGFR) ≥25–≤90 mL/min/1.73 m2, or UACR ≥300–≤5000 mg/g and eGFR ≥60 mL/min/1.73 m2, were randomized to finerenone or placebo. The primary cardiovascular composite outcome was time to cardiovascular death, non-fatal myocardial infarction, non-fatal stroke, or hospitalization for heart failure. The secondary kidney composite outcome was time to kidney failure, sustained eGFR decline ≥40% from baseline, or kidney-related death.

A total of 325 Chinese patients were included. Finerenone resulted in a numerical decrease in the risk of the cardiovascular composite outcome (hazard ratio 0.91; 95% confidence interval 0.50–1.67) and a significantly reduced risk of the key secondary kidney outcome (hazard ratio 0.48; 95% confidence interval 0.29–0.79; p = 0.0029). The incidence of investigator-reported hyperkalemia was high across both treatment arms. Nevertheless, the incidence of hyperkalemia leading to hospitalization and treatment discontinuation was low across treatment arms.

Finerenone significantly reduced the composite kidney outcome, showed a trend to reduce cardiovascular outcomes, and demonstrated an acceptable safety profile in Chinese patients.

## Linked entities

- **Chemicals:** finerenone (PubChem CID 24993045)
- **Diseases:** type 2 diabetes (MONDO:0005148), chronic kidney disease (MONDO:0005300), cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, NR3C2 (nuclear receptor subfamily 3 group C member 2) [NCBI Gene 4306] {aka MCR, MLR, MR, NR3C2VIT}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** CV (MESH:D002318), diabetic retinopathy (MESH:D003930), CKD (MESH:D051436), T2D (MESH:D003924), kidney failure (MESH:D051437), microvascular complications (OMIM:603933), stroke (MESH:D020521), death (MESH:D003643), kidney complications (MESH:D007674), fibrosis (MESH:D005355), inflammation (MESH:D007249), emergent (MESH:D004630), HHF (MESH:D006333), myocardial infarction (MESH:D009203), Hyperkalemia (MESH:D006947), Diabetic Kidney Disease (MESH:D003928), Diabetes (MESH:D003920), albuminuria (MESH:D000419), CKD stage 1 or 2 (MESH:D007676)
- **Chemicals:** FInerenone (MESH:C576501), DDP-4 (-), alcohol (MESH:D000438), biguanides (MESH:D001645), potassium (MESH:D011188), creatinine (MESH:D003404), insulin (MESH:D007328)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12074935/full.md

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Source: https://tomesphere.com/paper/PMC12074935